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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1150186 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
: S: N- h% w2 w% c8 o  p& v3 G4 ZNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
% b( }4 {7 _$ b! x7 U4 P+ Author Affiliations
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  {9 b3 K; _* I! S9 R1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 2 g3 A" S+ K8 X  ?
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 5 e6 ?- E, J8 X; }
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 8 j2 \& l0 k, H3 j& m2 x9 |9 u9 Y
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan & _* k1 Q" {7 U  z9 v) ~
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 8 m3 `, l- S8 @& H
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan . A$ t- w" Z; [, S) \
7Kinki University School of Medicine, Osaka 589-8511, Japan 4 A+ z0 j7 l9 \  g; J$ F
8Izumi Municipal Hospital, Osaka 594-0071, Japan ' d3 ?+ ?/ I) c8 z' G& S& x: B0 \
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
* N8 F5 L' ]! j% qCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp % u0 E. W$ ]+ e5 i" f  A
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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5 U5 l, [) l/ a/ U' s7 y! v. cAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
- W$ g( b1 q& B- b: f" V9 `
) U- J3 h9 _& r, @  F" mAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
. m; d% A9 }( f2 M; F" l- y4 o  Y3 B( G) S9 |3 E+ y' R& e
Published online on: Thursday, December 1, 2011
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7 V4 E/ H1 k2 nDoi: 10.3892/ol.2011.507
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Pages: 405-410
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Abstract:9 R# m" r  U4 g2 l
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
0 L) l+ y/ L1 L$ ?4 w( _F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 + x& p& ^4 |% L9 ~, \6 _
+ Author Affiliations% H6 Z' H7 q" J; m; a5 W6 B
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 3 r" z' n. T9 b' X  G/ y
2Department of Thoracic Surgery, Kyoto University, Kyoto
- N+ C' x: D6 Q+ f3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
& g8 e9 @" S2 J) [! T3 X- @&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
/ H: W% I* C9 }$ ~$ K  \Received September 3, 2010.
- [# A5 Q/ L; `# Y/ X, K6 ]Revision received November 11, 2010.
2 |9 |1 R2 B9 zAccepted November 17, 2010. ) |# G) G$ P. x+ R6 g2 t& y5 g
Abstract/ \- |, [: o, Y+ Z/ j7 I5 _
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. ' a- i4 T# y9 ?
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
" s; \( n% @5 ?5 l8 U: GResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. : z  W$ H- J, Z9 C
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
' n/ `$ Z5 E& K" i7 _今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?6 Y, L5 r- J7 Z
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
- @5 l2 X9 ~2 {8 Zhttp://clinicaltrials.gov/ct2/show/NCT01523587' H8 l# I7 [3 @! P

6 _# t% K1 C1 H1 x1 @* u0 \6 a$ b4 x) dBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
  ^9 {, f7 L6 Y6 ~+ n, Mhttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 " J4 I5 x/ g  Q& r. L. [% T
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。& M, h1 h$ M5 {* ~! P! E
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
6 A3 Q: c5 M% s* R2 H# g从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。3 B$ i6 d/ G- w. I( S3 k3 v
至今为止,未出 ...
) _0 K" m: R2 d5 b* u" b9 U
没有副作用是第一追求,效果显著是第二追求。
7 ~: v' G. g" `8 X  `  u8 V8 f不错。

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